Regulated production of a peroxisome proliferator-activated receptor-gamma ligand during an early phase of adipocyte differentiation in 3T3-L1 adipocytes

• Published in: The Journal of biological chemistry Vol. 279; no. 34; pp. 36093 - 36102
• Main Authors: Tzameli, Iphigenia, Fang, Hui, Ollero, Mario, Shi, Hang, Hamm, Jonathan K, Kievit, Paul, Hollenberg, Anthony N, Flier, Jeffrey S
• Format: Journal Article
• Language: English
• Published: United States 20-08-2004
• Subjects: 3T3-L1 Cells; Adipocytes - cytology; Adipocytes - physiology; Animals; beta-Galactosidase - physiology; Binding Sites; Cell Differentiation - physiology; Ligands; Mice; PPAR gamma - physiology; Signal Transduction
• ISSN: 0021-9258
• DOI: 10.1074/jbc.M405346200

Peroxisome proliferator-activated receptor-gamma (PPARgamma) is a nuclear hormone receptor that is critical for adipogenesis and insulin sensitivity. Ligands for PPARgamma include some polyunsaturated fatty acids and prostanoids and the synthetic high affinity antidiabetic agents thiazolidinediones. However, the identity of a biologically relevant endogenous PPARgamma ligand is unknown, and limited insight exists into the factors that may regulate production of endogenous PPARgamma ligands during adipocyte development. To address this question, we created a line of 3T3-L1 preadipocytes that carry a beta-galactosidase-based PPARgamma ligand-sensing vector system. In this system, induction of adipogenesis resulted in elevated beta-galactosidase activity that signifies activation of PPARgamma via its ligand-binding domain (LBD) and suggests generation and/or accumulation of a ligand moiety. The putative endogenous ligand appeared early in adipogenesis in response to increases in cAMP, accumulated in the medium, and dissipated later in adipogenesis. Organically extracted and high pressure liquid chromatography-fractionated conditioned media from differentiating cells, but not from mature adipocytes, were enriched in this activity. One or more components within the organic extract activated PPARgamma through interaction with its LBD, induced lipid accumulation in 3T3-L1 cells as efficiently as the differentiation mixture, and competed for binding of rosiglitazone to the LBD of PPARgamma. The active species appears to be different from other PPARgamma ligands identified previously. Our findings suggest that a novel biologically relevant PPARgamma ligand is transiently produced in 3T3-L1 cells during adipogenesis.